esv991335
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Pang et al. 2010
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 191 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 196 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 79 SVs from 11 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv991335 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 236,390,943 | 236,390,943 |
| esv991335 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 236,554,243 | 236,554,243 |
| esv991335 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 234,620,866 | 234,620,866 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3585997 | Remapped | Perfect | NC_000001.11:g.236 390943_236390944in s13 | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 236,390,943 | 236,390,943 |
| essv3585997 | Remapped | Perfect | NC_000001.10:g.236 554243_236554244in s13 | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 236,554,243 | 236,554,243 |
| essv3585997 | Submitted genomic | NC_000001.9:g.2346 20866_234620867ins 13 | NCBI36 (hg18) | NC_000001.9 | Chr1 | 234,620,866 | 234,620,866 |